Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia von Taniguchi‐Ikeda, M., Morisada, N., Inagaki, H., Ouchi, Y., Takami, Y., Tachikawa, M., Satake, W., Kobayashi, K., Tsuneishi, S., Takada, S., Yamaguchi, H., Nagase, H., Nozu, K., Okamoto, N., Nishio, H., Toda, T., Morioka, I., Wada, H., Kurahashi, H., Iijima, K.

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Disappearance of glomerular IgA deposits in childhood IgA nephropathy showing diffuse mesangial proliferation after 2 years of combination/prednisolone therapy von SHIMA, Yuko, NAKANISHI, Koichi, KAMEI, Koichi, TOGAWA, Hiroko, NOZU, Kandai, TANAKA, Ryojiro, SASAKI, Satoshi, IIJIMA, Kazumoto, YOSHIKAWA, Norishige

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Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome von Krol, Rafal Przybyslaw, Nozu, Kandai, Nakanishi, Koichi, Iijima, Kazumoto, Takeshima, Yasuhiro, Fu, Xue Jun, Nozu, Yoshimi, Kaito, Hiroshi, Kanda, Kyoko, Matsuo, Masafumi, Yoshikawa, Norishige

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Usefulness of automatic detection of fragmented red cells using a hematology analyzer for diagnosis of thrombotic microangiopathy von Saigo, K., Jiang, M., Tanaka, C., Fujimoto, K., Kobayashi, A., Nozu, K., Iijima, K., Ryo, R., Sugimoto, T., Imoto, S., Kumagai, S.

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Risk factors for persistent proteinuria after a 2-year combination therapy for severe childhood IgA nephropathy von Kamei, Koichi, Nakanishi, Koichi, Ito, Shuichi, Ishikura, Kenji, Hataya, Hiroshi, Honda, Masataka, Nozu, Kandai, Iijima, Kazumoto, Shima, Yuko, Yoshikawa, Norishige

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Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome von Nozu, Kandai, Iijima, Kazumoto, Fujisawa, Masato, Nakagawa, Atsuko, Yoshikawa, Norishige, Matsuo, Masafumi

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Two-Year Outcome of the ISKDC Regimen and Frequent-Relapsing Risk in Children with Idiopathic Nephrotic Syndrome von Nakanishi, Koichi, Iijima, Kazumoto, Ishikura, Kenji, Hataya, Hiroshi, Nakazato, Hitoshi, Sasaki, Satoshi, Honda, Masataka, Yoshikawa, Norishige

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Risk factors for cyclosporine-induced tubulointerstitial lesions in children with minimal change nephrotic syndrome von Iijima, Kazumoto, Hamahira, Kiyoshi, Tanaka, Ryojiro, Kobayashi, Akiko, Nozu, Kandai, Nakamura, Hajime, Yoshikawa, Norishige

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Blockade of Alternative Complement Pathway in Dense Deposit Disease von Berthe-Aucejo, Aurore, Deschênes, Georges, Frémeaux-Bacchi, Véronique, Perrier-Cornet, Emilia, Sacquépée, Mathieu, Fila, Marc, Peuchmaur, Michel

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Microsporidia Infection in a Mexican Kidney Transplant Recipient von Hernández-Rodríguez, Oscar Xavier, Alvarez-Torres, Octavio, Ofelia Uribe-Uribe, Norma

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EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions von Okada, Michiyo, Fujimaru, Rika, Morimoto, Noriko, Satomura, Kenichi, Kaku, Yoshikazu, Tsuzuki, Kazuo, Nozu, Kandai, Okuyama, Torayuki, Iijima, Kazumoto

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Paediatric nephrology - A von Okamoto, S., Sakama, T., Nakamura, S., Niimura, F., Sahin, S., Ertan, P., Evrengul, H., Horasan, G., Dede, B., Berdeli, A., Yildiz, N., Cicek Deniz, N., Asadov, R., Yucelten, D., Alpay, H., Prado, G., Schoeneman, M., Mongia, A., Paudyal, B., Feygina, V., Norin, A., Hochman, D., Tawadrous, H., Bansilal, V., Topaloglu, R., Gulhan, B., Bilginer, Y., Celebi Tayfur, A., Yildiz, C., Ozaltin, F., Duzova, A., Ozen, S., Aki, T., Besbas, N., Komaki, F., Hamasaki, Y., Ishikura, K., Hamada, R., Sakai, T., Hataya, H., Ogata, K., Fukuzawa, R., Ando, T., Honda, M., Malke, A., Silska-Dittmar, M., Soltysiak, J., Blumczynski, A., Ostalska-Nowicka, D., Zachwieja, J., Tabel, Y., Oncul, M., Elmas, A., Kavaz, A., Ozcakar, Z. B., Bulum, B., Ekim, M., Yalcinkaya, F., Prikhodina, L., Turpitko, O., Dlin, V., Gheith, O., Alotaibi, T., Nampoory, N., Mosaad, A., Halim, M., Saied, T., Abou Ateya, H., Adel, H., Mozarei, I., Neir, P., Uemura, O., Ito, S., Wada, N., Hattori, M., Ohashi, Y., Tanaka, R., Nakanishi, K., Kaneko, T., Golovachova, V., Odinets, Y., Laszki-Szczachor, K., Polak-Jonkisz, D., Sobieszczanska, M., Rusiecki, L., Zwolinska, D., Ninchoji, T., Kaitoh, H., Matsunoshita, N., Nozu, K., Yoshikawa, N., Iijima, K., Maglalang-Reed, O. M., Elises, J. S., Zamora, M. N. V., Pasco, P., Arejola-Tan, A., Alparslan, C., Dogan, S. M., Kose, E.

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Estradiol receptor-mediated regulation of steroidogenesis in gonadotropin-desensitized Leydig cells von Nozu, K, Dufau, M L, Catt, K J

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Cyclosporin A absorption profiles in children with nephrotic syndrome von Nozu, Kandai, Iijima, Kazumoto, Sakaeda, Toshiyuki, Okumura, Katsuhiko, Nakanishi, Koichi, Yoshikawa, Norishige, Honda, Masataka, Ikeda, Masahiro, Matsuo, Masafumi

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High-dose mizoribine treatment for adolescents with systemic lupus erythematosus von NOZU, KANDAI, IIJIMA, KAZUMOTO, KAMIOKA, ICHIRO, FUJITA, TERUO, YOSHIYA, KUNIHIKO, TANAKA, RYOJIRO, NAKANISHI, KOICHI, YOSHIKAWA, NORISHIGE, MATSUO, MASAFUMI

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A-20C angiotensinogen gene polymorphism and proteinuria in childhood IgA nephropathy von Nakanishi, Koichi, Sako, Mayumi, Yata, Nahoko, Aoyagi, Noriyuki, Nozu, Kandai, Tanaka, Ryojiro, Iijima, Kazumoto, Yoshikawa, Norishige

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Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated? von Fujita, Teruo, Nozu, Kandai, Iijima, Kazumoto, Kamioka, Ichiro, Yoshiya, Kunihiko, Tanaka, Ryojiro, Hamahira, Kiyoshi, Nakanishi, Koichi, Yoshikawa, Norishige, Matsuo, Masafumi

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Modulation of Leydig cell androgen biosynthesis and cytochrome P-450 levels during estrogen treatment and human chorionic gonadotropin-induced desensitization von Nozu, K, Matsuura, S, Catt, K J, Dufau, M L

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Hormonal modulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in gonadotropin-stimulated and -desensitized testicular Leydig cells von Charreau, E H, Calvo, J C, Nozu, K, Pignataro, O, Catt, K J, Dufau, M L

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Hyperthermic Effects on DNA Repair of UV-irradiated Dictyostelium Discoideum von Ohnishi, T., Iwata, K., Hamada, N., Nozu, K.

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